A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789905



Internal ID21235243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134055478..134055478hg38UCSC Ensembl
chr11:133925373..133925373hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13690910, nssv13680853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789905
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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